Spinal Implant Apparatuses and Methods of Implanting and Using Same

ABSTRACT

An adjustable spinal implant device, comprising: a sliding portion provided with a tongue; and, a non-sliding portion provided with a slot adapted for receipt of the tongue; wherein the tongue is slidably and rotatably positioned within the slot.

RELATED APPLICATIONS

This application is related to an application entitled “Spring ScrewApparatuses and Methods of Using Same”, filed on the same date of Dec.17, 2010 in the United States Patent and Trademark Office, with the samenamed inventors, the disclosure of which is incorporated herein byreference.

FIELD AND BACKGROUND OF THE INVENTION

The present invention relates to spinal implants and methods ofimplantation and use of the implants in general, and more particularlyto spinal implants for replacing at least the spinous process and/or foroperating as cross-links and methods relating to same.

Referring to FIG. 1 a perspective view of the spinal anatomy is shown.Briefly, the spinal column 100 is divided into five sections beginningwith the cervical section 102, the thoracic section 104, the lumbarsection 106, the sacrum 108 and finally the coccyx 110. Each majorsection (cervical 102, thoracic 104, lumbar 106) is made up ofindividual bones called vertebrae. In a conventional spinalconfiguration, there are 7 cervical vertebrae, 12 thoracic vertebrae,and 5 lumbar vertebrae.

An individual vertebra is made up of several anatomical features.Generally, each vertebra of the three major sections has the same majorfeatures. FIG. 2 is a cross-sectional view of a thoracic vertebra 200.The body 202 of the vertebra is the primary area of weight bearing andprovides a resting place for the fibrous discs which separate each ofthe vertebrae. The lamina 208 covers the spinal canal, the large openingin the center of the vertebra through which the spinal cord passes, andthe neural foramen, where the spinal nerves exit. The spinous process212 is the bone that can be felt when running a hand down a person'sback. The paired transverse processes 204 are oriented 90 degrees to thespinous process 212 and provide attachment for back muscles. Pedicles206 connect the transverse processes 204 to the body 202. Locatedbetween the transverse processes 204 and the laminae 208 are superiorarticular processes 210.

Often times, one or some of the major vertebral features is removed toeffectuate treatment of a patient, for example in a laminectomy at leasta portion of a lamina 208 is removed. It is not unusual for some or allof the spinous process 212, the laminae 208, the superior articularprocesses 210 or even the transverse processes 204 to be removed in asurgical procedure.

U.S. Pat. Nos. 7,566,345, 6,902,580 and 6,419,703 to Fallin, et al., thedisclosures of which are incorporated herein by reference, describeprosthetic replacements for a posterior element of a vertebra comprisingportions that replace the natural lamina and the four natural facets.The prosthetic replacements may also include portions that replace oneor more of the natural spinous process and the two natural transverseprocesses. If desired, the prosthesis replacements may also replace thenatural pedicles. Methods for replacing a posterior element of avertebra are also provided.

United States Patent Application Publication No. US 2005/0033434 toBerry, the disclosure of which is incorporated herein by reference,describes a prosthetic device for interposition in a space left by oneor more excised vertebral posterior structures. The prosthetic devicecomprises a lamina bridge having an inferior portion for replacing anexcised lamina; at least one inferior facet replacement device,connected to the inferior portion of the lamina bridge, to replace anexcised inferior articular process; and at least one superior facetreplacement device to replace an excised superior articular process. Theat least one superior facet replacement device articulates with the atleast one inferior facet replacement device.

United States Patent Application Publication No. US 2005/0010291 toStinson, et al., the disclosure of which is incorporated herein byreference, describes cephalad and caudal vertebral facet jointprostheses and methods of use. The cephalad prostheses are adapted andconfigured to be attached to a lamina portion of a vertebra withoutblocking a pedicle portion of the cephalad vertebra. In someembodiments, the prosthesis is attached with a non-invasive supportmember, such as a clamp. In other embodiments, a translaminar screw maybe used for additional fixation.

PCT Application Publication No. WO 99/23963 to Senegas, the disclosureof which is incorporated herein by reference, describes a cervicalvertebra implant comprising two branches adapted to extend respectivelysubstantially along two cervical blades of a common cervical vertebraspaced from each other after osteotomy of the blades, and a rigid bodylinking the two branches.

SUMMARY OF THE INVENTION

An aspect of the present invention relates to providing a spinal implantdevice which is adjustable for adapting the implant to a variety ofindividual patient conditions and/or anatomies. In some embodiments ofthe invention, the implant is width adjustable by sliding at least aportion of the implant generally perpendicular to the spinal column toadjust the width of the implant to match the anatomical features of aparticular vertebra. Additionally, optionally and/or alternatively, thespinal implant is orientation adjustable by rotating at least a portionof the implant around a vertical axis extending anteriorly/posteriorlyas the patient is laying face down on a table. In some embodiments ofthe invention, the at least a portion of the implant that can be rotatedis used to accommodate crosslink rods and/or to ease implantation.Optionally, rotation is used to attach the implant to non-parallelcross-link rods.

In an exemplary embodiment of the invention, the spinal implant iscomprised of at least one of a prosthetic spinous process and/or atleast one prosthetic lamina. In an embodiment of the invention, at leastone hole is provided to the prosthetic spinous process for attachment ofsoft tissues, for example muscle.

In an embodiment of the invention, at least one loop is located on alateral aspect of the prosthetic lamina. In an exemplary embodiment ofthe invention, at least one loop is used to secure the spinal implant toa vertebra by passing a screw therethrough and tightening the screw to asite on the vertebra, such as a lateral mass, facet, or pedicle.

In an embodiment of the invention, the spinal implant is adapted to beused with and/or as a part of a cross-link system. In some exemplaryembodiments of the invention, the rod is a rod of a fusion construct orcross-linking system. By using a cam screw provided with a taperingcambered surface, the implant is secured to and/or accommodatesdifferent rod sizes (e.g. circumferences) without having to use adifferent screw and/or clamp for each possible size just by turning thescrew until the taper of the cambered surface matches the size of therod. In an embodiment of the invention, markings are provided to thescrew and/or implant to indicate “open” and/or “closed” or “locked”and/or “unlocked” positions.

In an embodiment of the invention, the spinal implants, whileadjustable, are offered in more than one size. For example, due to thedifferences in overall size between the cervical, thoracic and lumbarsection of the spine, sizes tailored for these three sections of thespine are optionally offered, which are additionally adjustable forwidth as described elsewhere herein. In some embodiments of theinvention, only two basic sizes are offered, thoracolumbar (thoracic andlumbar combined) and cervical.

A further aspect of the present invention relates to a cross-linkingsystem including at least one of a spinal implant device and a cam screwprovided with a tapered, cambered surface which is usable with a rangeof fusion rod sizes. In an embodiment of the invention, the spinalimplant is provided with at least one screw hole to accommodate theinsertion and/or rotation of the cam screw therein. In operation, withthe cam screw inserted into the screw hole, a rotation tool interfaceend of the cam screw is positioned opposite a cam end of the screw suchthat the rotation tool interface end is accessible to an attendingmedical professional for applying rotational force, whereas the cam endis positioned proximal to a fusion rod secured to at least one vertebra.

In some embodiments of the invention, the spinal implant device isadjustable to a particular vertebra's anatomy. Optionally, the spinalimplant is width adjustable. Optionally, additionally and/oralternatively, the spinal implant is orientation adjustable.

In an embodiment of the invention, a plurality of spinal implant devicesare attached to the same at least one fusion rod to provide mechanicalstability over a plurality of vertebrae. Optionally, at least two of thevertebrae are consecutive. Optionally, at least two of the vertebrae arenot consecutive.

In an embodiment of the invention, the device is adapted to attach to afusion rod at or near the spinous process. Optionally, the fusion rod ator around the spinous process is the third fusion rod attached to thedevice. In an embodiment of the invention, a plurality of fusion rodsizes are accommodated, for example by providing a cam screw, such asthose described elsewhere herein to the spinous process for securing therod in place. Optionally, a clamp-like mechanism is used to secure therod to the device. Optionally, a tightening screw traps the rod againstan immovable bracket to secure the rod. In some embodiments of theinvention, the rod attached at or near the spinous process is attachedin the same location on an adjacent implant, that is on an implant on avertebra adjacent. Optionally, the rod is attached to an implant on anon-adjacent vertebra.

A further aspect of the present invention relates to a method ofimplanting a spinal implant by adjusting the spinal implant to adapt theimplant to a particular patient's condition and/or anatomy. Optionally,adjusting includes sliding at least a portion of the implant to adapt.Optionally, adjusting includes rotating at least a portion of theimplant to adapt. In an embodiment of the invention, the spinal implantis adjusted for width by sliding a portion of the implant to make theoverall implant wider or narrower. In an embodiment of the invention,the spinal implant is adjusted for orientation by rotating at least aportion of the implant with respect to another portion of the implant.

A tightening screw is used to control the sliding portion of the implantfrom sliding relative to the non-sliding portion of the implant and/orto prohibit rotation of at least a portion of the implant with respectto another portion of the implant, in an embodiment of the invention. Inan embodiment of the invention, control of the sliding and/or rotatingis variable across a spectrum from moving freely to locked depending onthe degree the screw is tightened. In an embodiment of the invention,the implant is fastened to a vertebra. Optionally, screws fasten theimplant directly to a vertebra. The screws can be placed in a lateralmass, facet, lamina and/or pedicle of the bone, in an embodiment of theinvention. Additionally, optionally and/or alternatively, the implant isconnected to a cross-link apparatus wherein the cross-link apparatus isconnected to at least one vertebra.

A further aspect of the present invention relates to a method ofconnecting a spinal implant device to at least one of a plurality ofsizes of fusion rod. In an embodiment of the invention, at least onecross-link rod is attached to a plurality of vertebrae. Optionally, atleast two of the vertebrae are consecutive. Optionally, at least two ofthe vertebrae are not consecutive.

In an embodiment of the invention, at least one spinal implant is placedover the pre-attached fusion rod using the adjustment features of thespinal implant, including sliding and/or rotating. In an embodiment ofthe invention, when the spinal implant is placed over the fusion rod, acam screw which is provided to the spinal implant is in the “open”position, wherein the tapered, cambered surface of the cam screw is notyet engaged with the rod.

The spinal implant is connected to at least one fusion rod by tightening(i.e. rotating) the cam screw so that the tapered, cambered surfaceengages the rod. As the cam screw is turned in the tightening direction,the taper of the cambered surface gradually narrows. The camberedsurface in contact with the rod therefore narrows as the cam screw isturned to accommodate rods of smaller and smaller circumference. In anembodiment of the invention, the cam screw is turned until the taper ofthe cambered surface matches the rod and the rod becomes immobilizedbetween the cam screw and a bracket of the spinal implant. Optionally,the cam screw is rotated to a locked position.

In an embodiment of the invention, placing, tightening and connectingare repeated as necessary depending on the number of spinal implantsbeing attached to the at least one fusion rod.

There is therefore provided in accordance with an embodiment of theinvention, an adjustable spinal implant device, comprising: a slidingportion provided with a tongue; and, a non-sliding portion provided witha slot adapted for receipt of the tongue; wherein the tongue is slidablyand rotatably positioned within the slot.

In an embodiment of the invention, a screw hole is provided to thenon-sliding portion adapted for receipt of a tightening screw therein.

In an embodiment of the invention, the tightening screw defines an axisfor rotation of the sliding and non-sliding portions with respect toeach other.

In an embodiment of the invention, a sliding track located within thetongue is adapted for receipt of the tightening screw.

In an embodiment of the invention, the device further comprises aprosthetic spinous process. Optionally, the device further comprises atleast one soft tissue attachment hole located on the prosthetic spinousprocess.

In an embodiment of the invention, the device further comprises at leastone loop adapted for receipt of a bone screw therethrough on theanterior of at least one of the sliding portion and the non-slidingportion.

In an embodiment of the invention, the device further comprises at leastone cam screw bracket adapted for receipt of a cam screw therethrough onthe anterior of at least one of the sliding portion and the non-slidingportion. In some embodiments of the invention, the cam screw is providedwith a cam retaining pin groove. Optionally, the cam retaining pingroove is provided with at least one locking point.

In an embodiment of the invention, the cam screw is provided with atapered and cambered surface. Optionally, the tapered and camberedsurface tapers from large to small in the tightening rotationaldirection. Optionally, the tapered and cambered surface is a counterpartto the outer circumference of a plurality of fusion rods.

In an embodiment of the invention, the spinal implant is between 20.0 mmto 45.0 mm in the anterior/posterior axis, between 10.0 mm to 30.0 mm inthe superior/inferior axis, and between 25.0 mm to 55.0 mm in thedextro/sinistral axis. In some embodiments of the invention, the spinalimplant is adapted for use with cervical vertebrae and is between 20.0mm to 30.0 mm in the anterior/posterior axis, 10.0 mm to 20.0 mm in thesuperior/inferior axis and 25.0 mm to 35.0 mm in the dextro/sinistralaxis. In some embodiments of the invention, spinal implant is adaptedfor use with thoracic vertebrae and is 25.0 mm to 35.0 mm in theanterior/posterior axis, 15.0 mm to 25.0 mm in the superior/inferioraxis and 35.0 mm to 45.0 mm in the dextro/sinistral axis. In someembodiments of the invention, the spinal implant is adapted for use withlumbar vertebrae and is 35.0 mm to 45.0 mm in the anterior/posterioraxis, 20.0 mm to 30.0 mm in the superior/inferior axis and 45.0 mm to55.0 mm in the dextro/sinistral axis. In some embodiments of theinvention, the spinal implant is adapted for use with the thoracolumbarsection of the spine and is between 25.0 mm to 45.0 mm in theanterior/posterior axis, between 15.0 mm to 30.0 mm in thesuperior/inferior axis and between 35.0 mm to 55.0 mm in thedextro/sinistral axis.

In an embodiment of the invention, the implant is at least partiallyconstructed of titanium.

In an embodiment of the invention, the implant is at least partiallyconstructed of stainless steel.

In an embodiment of the invention, the implant is at least partiallyconstructed of polyetheretherketone.

There is further provided in accordance with an exemplary embodiment ofthe invention, a cross-link system adapted for use with a plurality offusion rod sizes, comprising: at least one fusion rod; at least onespinal implant provided with at least one bracket located on theanterior of the implant; and, at least one cam screw inserted throughthe at least one bracket and provided with a tapered and camberedsurface wherein the cambered surface tapers across a spectrumcorresponding to a plurality of outer circumferences of a plurality offusion rods.

In an embodiment of the invention, the cambered surface is adapted toselectively trap the at least one fusion rod between the cam screw andthe bracket.

In an embodiment of the invention, the at least one spinal implant isprovided with two portions which are slidable and rotatable in relationto each other to assist with positioning the cam screw against the atleast one fusion rod.

In an embodiment of the invention, the taper of the cambered surfacenarrows in the tightening rotational direction.

In an embodiment of the invention, the plurality of outer circumferencesof a plurality of fusion rods ranges from 3.3 mm to 5.0 mm.

There is further provided in accordance with an exemplary embodiment ofthe invention, a locking cam screw, comprising, a cambered surface on acam end; and, a retaining pin groove located around the circumference ofa rotation tool interface end opposite the cam end on the cam screw;wherein the retaining pin groove is provided with at least one lockingpoint adapted to pass a retaining pin therethrough in at least atightening direction.

In an embodiment of the invention, the at least one locking point is anarrowing of the retaining pin groove.

In an embodiment of the invention, the position of the at least onelocking point in the retaining pin groove relates to the rotationaldistance of cam screw needed to match the cambered surface to the outercircumference of a cross-link rod

In an embodiment of the invention, the retaining pin groove is providedwith a plurality of locking points. In some embodiments of theinvention, each of the plurality of locking points corresponds to arotational distance needed to match the cambered surface to an outercircumference of a cross-link rod.

There is further provided in accordance with an exemplary embodiment ofthe invention, a method for implanting a spinal implant at an implantsite, comprising: adjusting the spinal implant to the implant site by atleast one of sliding and rotating at least a first portion with respectto a second portion of the implant; and, securing the spinal implant tothe implant site.

In an embodiment of the invention, the method further comprisesfastening at least one cross-link rod so that is traverses the implantsite. In some embodiments of the invention, the method further comprisesconnecting the implant to the at least one cross-link rod.

In an embodiment of the invention, the implant site includes at leastone of a pedicle, a facet, a lateral mass and a lamina.

In an embodiment of the invention, the method further comprisestightening a screw to selectively limit at least one of sliding androtating.

There is further provided in accordance with an exemplary embodiment ofthe invention, a method for connecting at least one spinal implant to atleast one of a plurality of cross-link rods in a cross-link arrangement,comprising: connecting at least one cross-link rod to a plurality ofvertebrae; placing at least one spinal implant over the at least onecross-link rod wherein a cambered surface of a cam screw provided to thespinal implant is in the open position and proximal to the cross-linkrod; and, tightening the cambered and tapered cam screw so that itengages the cross-link rod and pins it between the cam screw and thespinal implant.

In an embodiment of the invention, the method further comprisesrepeating placing and tightening for additional spinal implants andcross-link rods.

In an embodiment of the invention, the placing includes at least one ofsliding and rotating at least a portion of the spinal implant.

In an embodiment of the invention, the wherein at least two consecutivevertebrae are connected.

In an embodiment of the invention, the at least two non-consecutivevertebrae are connected.

In an embodiment of the invention, the method further comprises lockingthe cam screw to inhibit back rotation of the cam screw.

These and other features and their advantages will be readily apparentto those skilled in the art of spinal implants from a careful reading ofthe Detailed Description of Exemplary Embodiments, accompanied by thefollowing drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

Embodiments of the invention are herein described, by way of exampleonly, with reference to the accompanying drawings. In this regard, thedescription taken along with the drawings makes apparent to thoseskilled in the art how embodiments of the invention may be practiced. Itshould also be understood that drawings may not be to scale. In thefigures,

FIG. 1 is a perspective view of the spinal anatomy;

FIG. 2 is a cross-sectional view of a lumbar vertebra;

FIG. 3A is a perspective view of a sliding spinal implant with aprosthetic spinous process in a narrow configuration, in accordance withan exemplary embodiment of the invention;

FIG. 3B is a perspective view of a sliding spinal implant with aprosthetic spinous process in at least a partially open or wideconfiguration, in accordance with an exemplary embodiment of theinvention;

FIG. 4 is a top view of a sliding spinal implant with a prostheticspinous process, in accordance with an exemplary embodiment of theinvention;

FIG. 5A is a perspective view of a spinal implant with opposingcomponents rotating about a vertical axis, in accordance with anexemplary embodiment of the invention;

FIG. 5B is a top view of a spinal implant with opposing componentsrotating about a vertical axis, in accordance with an exemplaryembodiment of the invention;

FIG. 5C is a cross-sectional view of a portion of a spinal implant withopposing components capable of rotating about a vertical axis, inaccordance with an exemplary embodiment of the invention;

FIG. 6 is an exploded view of a spinal implant with a cam screwarrangement for interfacing with at least one rod of a spinal implantsystem, in accordance with an exemplary embodiment of the invention;

FIG. 7A is a perspective view of an implant with a cam screw arrangementfor interfacing with a rod of a cross-link system, in accordance with anexemplary embodiment of the invention;

FIG. 7B is a side view of the implant of FIG. 7A showing where thecross-sectional view of FIG. 7C is taken from, in accordance with anexemplary embodiment of the invention;

FIG. 7C is a cross-sectional view of the implant of FIG. 7A, inaccordance with an exemplary embodiment of the invention;

FIG. 8 is a perspective view of a cam screw used in a cam screwarrangement for interfacing with a rod of a cross-link system, inaccordance with an exemplary embodiment of the invention;

FIG. 9A is a side view of an altered spinal column with a spinal implantimplanted thereon, in accordance with an exemplary embodiment of theinvention;

FIG. 9B is a side view of an altered spinal column with a cross-linkedspinal implants implanted thereon, in accordance with an exemplaryembodiment of the invention;

FIGS. 10A-C are cross-sectional views of altered cervical, thoracic andlumbar vertebrae, respectively, with a spinal implant implanted thereon,in accordance with an exemplary embodiment of the invention;

FIG. 11 is a flowchart showing a method of implanting a spinal implant,in accordance with an exemplary embodiment of the invention; and,

FIG. 12 is a flowchart showing a method for attaching a spinal implantto any one of a plurality of fusion rod sizes, in accordance with anexemplary embodiment of the invention.

DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTS

Exemplary embodiments of spinal implants are described herein. In someembodiments of the invention, spinal implants are used to reconstructdamaged and/or defective spinal structures, particularly the spinousprocess and/or the laminae. In an embodiment of the invention, a spinalimplant is used as a prosthesis for vertebrae in any, some or all of thecervical 102, thoracic 104, lumbar 106 or sacral 108 sections of thespinal column 100. Additionally, alternatively and/or optionally, aspinal implant is used as a component in a cross-link system for linkingtwo or more vertebrae together, in an embodiment of the invention.

In an embodiment of the invention, spinal implant 300 is offered in aplurality of configurations adapted for use in the cervical 102,thoracic 104, and/or lumbar 106 sections of the spine. Optionally, asingle configuration is adapted for use with both the thoracic andlumbar sections. Optionally, at least one of the configurations isoffered in a plurality of sizes, for example the thoracolumbarconfiguration could be offered in a “large”, “medium” and/or a “small”size. In an embodiment of the invention, an implant is sized for use byaltering the dimensions in the anterior/posterior axis (“depth”), thesuper/inferior axis (“height”) and/or the dextro/sinistral (“width”)axis. For example, spinal implants described herein are sized between20.0 mm to 45.0 mm in the anterior/posterior axis, in an embodiment ofthe invention. Spinal implants described herein are sized 10.0 mm to30.0 mm in the superior/inferior axis, in some embodiments of theinvention. In some embodiments of the invention, spinal implantsdescribed herein are sized between 25.0 mm to 55.0 mm in thedextro/sinistral axis. It should be understood that these numbers are byway of example only and that sizes and/or dimensions given herein arenot necessarily those of every embodiment.

In an embodiment of the invention, the spinal implant adapted for usewith the cervical section of the spine is approximately 20.0 mm to 30.0mm in depth (from anterior to posterior when the device is implanted),10.0 mm to 20.0 mm in height (from superior to inferior when the deviceis implanted) and 25.0 to 35.0 mm in width in the dextro/sinistral axis.

In an embodiment of the invention, the spinal implant adapted for usewith the thoracic section of the spine is approximately 25.0 mm to 35.0mm in depth, 15.0 mm to 25.0 mm in height and 35.0 mm to 45.0 mm inwidth.

In some embodiments of the invention, a spinal implant adapted for usewith the lumbar section of the spine is approximately 35.0 mm to 45.0 mmin depth, 20.0 mm to 30.0 mm in height and 45.0 mm to 55.0 mm in width.

As described above, a single size and/or configuration could be usedwith the thoracolumbar section of the spine. These sizes would be in therange of 25.0 mm to 45.0 mm in depth; 15.0 mm to 30.0 mm in height, and35.0 mm to 55.0 mm in width, in an exemplary embodiment of theinvention.

In an embodiment of the invention, the spinal implant is widthadjustable by using a slidable portion of the implant, for example asshown and described with respect to FIGS. 3A and 3B, inter alia.Optionally, opposing components of the spinal implant are rotatablearound a vertical axis (from the perspective of the attending medicalprofessional when the patient is laying face down) extending in theanterior/posterior axis of the implant, for example as shown anddescribed with respect to FIGS. 4, and 5A-5C, inter alia.

Another feature of some embodiments of the invention relates to aplurality of interchangeable anterior portions which are used forconnecting the spinal implants to vertebrae and/or in a cross-linkingarrangement. Nearly all of the Figures show at least one embodiment forconnection, including loops (FIGS. 3A-3B, 4, 5A-5B), or brackets with acam screw (FIGS. 6, 7A-7C). It should be understood that some or all ofthese connection embodiments are adapted for use with any of the spinalimplants described herein and vice versa.

Referring to FIGS. 3A and 3B, in some embodiments of the invention, anon-sliding portion 304 and a sliding portion 312 are adapted tosimulate and/or replace the natural laminae 208 of the vertebra 200, inan embodiment of the invention. In some exemplary embodiments of theinvention, non-sliding portion 304 and sliding portion 312 also replacethe natural superior articular processes 210 extending from theprosthetic spinous process 302 to the transverse process 204 and/or thepedicle 206. In an embodiment of the invention, non-sliding portion 304and/or sliding portion 312 are adapted to provide more clearance betweenspinal implant 300 and the spinal cord and/or thecal sac (in the case ofthe lumbar section) located within the spinal column 100. For example,non-sliding portion 304 and/or sliding portion 312 are arched at leastas much as the natural portions of the vertebra being replaced.Optionally, non-sliding portion 304 and/or sliding portion 312 arearched more than the natural portions of the vertebra being replaced.

Spinal implant 300 is constructed of any material which is biocompatibleand which is mechanically capable of withstanding stresses ofcross-linking, for those embodiments of the invention which are used ina cross-linking arrangement. In some embodiments of the invention,spinal implant 300 is constructed of a metal, for example titanium. Insome exemplary embodiments of the invention, spinal implant 300 isconstructed of a polymer material, for example polyetheretherketone(PEEK). In an embodiment of the invention, the implant is constructedfrom any bio-compatible material rigid enough to function as at least aportion of a prosthetic lamina and/or spinous process and/or in across-link system.

Spinal implant 300 is intended to be adaptable to a variety of patientconditions and/or anatomies so that less device sizes are required to beon hand and/or manufactured in order to suit an individual patient'sneeds. In some embodiments of the invention, at least a portion of thespinal implant slides with respect at least another portion of theimplant in order to adjust the overall width (as used above in paragraph

with respect to “width”) of the implant allowing the implant to beadaptable to a variety of patient conditions and/or anatomies. FIG. 3Ashows a perspective view of a sliding spinal implant 300 with aprosthetic spinous process 302 in a narrow configuration, in accordancewith an exemplary embodiment of the invention. That is, in its narrowestconfiguration whereby the sliding portion 312 and the non-slidingportion 304 abut one another to create a configuration of the narrowestachievable width for implant 300. FIG. 3B, however, shows implant 300 atleast partially “open” or wider by taking advantage of the slidingfeature of the sliding portion 312 and the non-sliding portion 304counterparts in the direction of arrows 316. It should be understoodthat implant width is also adjustable when rotated, as described belowin more detail with respect to FIGS. 4, and 5A-5C.

In an embodiment of the invention, sliding portion 312 slides withrespect to non-sliding portion 304 of spinal implant 300 in order toincrease and/or decrease the overall width of spinal implant 300. It isnoted that “non-sliding” portion is used for nomenclature only and thatin practice it is possible that sliding portion 312 remains still whilenon-sliding portion 304 slides towards or away from sliding portion 312,or they both 304, 312 slide simultaneously. At least one screw hole 306is provided to spinal implant 300 which enables a tightening screw (notpictured) to be used to lock the spinal implant 300 width once thedesired width is achieved by sliding. In an embodiment of the invention,sliding portion 312 is provided with a tongue 318 which is adapted to beslidable within a slot 320 formed by non-sliding portion 304 for widthadjustment. In an embodiment of the invention, a track 314 is located ontongue 318 of sliding portion 312 to accommodate the tightening screwalong a range of lengths of spinal implant 300.

In some embodiments of the invention, the slide adjustable implant 300is adjustable by hand. In an embodiment of the invention, the slidingaction of the sliding portion 312 and/or non-sliding portion 304 withrespect to each other is controllable across a spectrum from slidingfreely to locked by the tightening screw which when fully tightenedstops the sliding portion from sliding relative to the non-slidingportion of the implant. Optionally, at least the sliding portion 312 isdemarcated for precise and/or accurate adjustment of the implant. Forexample, the sliding portion 312 is marked with pre-selected positionnumbers and/or an actual distance measurement indication. In anembodiment of the invention, the slide of the sliding portion 312 islocated near or at the intersection of the spinous process 302 (or wherethe spinous process would normally be) and the laminae. In someembodiments of the invention, sliding portion 312 is located on thespinous process 302 on the posterior side of the implant 300.

Screw hole 306 and track 314 are more clearly seen in FIG. 4, a top viewof sliding spinal implant 300 with a prosthetic spinous process 302, inaccordance with an exemplary embodiment of the invention. In anembodiment of the invention, the prosthetic spinous process 302 haslocated therein at least one hole 308 for attachment of soft tissues,for example muscle. In an embodiment of the invention, at least one loop310 is provided to spinal implant 300 which is adapted for receipt of apedicle and/or lateral mass screw therethrough. Optionally, the at leastone loop 310 is adapted for use with a spring screw as described inrelated application entitled Spring Screw Apparatus and Methods of Usingsame, filed on the same date as this application. In some embodiments ofthe invention, at least one loop 310 is located on the anterior portion(anatomically speaking) of spinal implant 300. In an embodiment of theinvention, locating loops 310 anteriorly allows for spinal implant 300to be attached to the spinal column through the loop 310.

Also visible in FIG. 4 is at least a part of the rotation wedge 402located on the non-sliding portion 304. Rotation wedge 402 is shown anddescribed in more detail with respect to FIGS. 5A-5C. Non-slidingportion 304 is adapted with rotation wedge 402 to allow rotation of thesliding portion 312 and the non-sliding portion 304 with respect to eachother.

FIG. 5A is a perspective view of spinal implant 300 with opposingcomponents 304, 312 rotating about a vertical axis 502, in accordancewith an exemplary embodiment of the invention. In an embodiment of theinvention, implant 300 is adjustable not only in width as describedabove but also in orientation whereby implant 300 is provided at least asecond degree of motion around vertical axis 502 (the first degree beingthe adjustable width) to accommodate for variations in spinal anatomyfrom patient to patient and/or from vertebra to vertebra. A screw or pinis nominally inserted into screw hole 306 mechanically defining thevertical axis 502 about which rotation occurs. In use, the screw or pinis also used to secure the implant 300 configuration for width and/orfor rotation, for example by screwing down to tighten the connectionbetween components 304, 312 and/or eventually prohibiting relativemovement between the two. Optionally, the securing is not permanent buttemporary, for example if adjustments need to be made to width and/orrotation at a later date.

FIG. 5B is a top view of a spinal implant with opposing components 304,312 rotating about vertical axis 502, in accordance with an exemplaryembodiment of the invention. Rotation about vertical axis 502 providesan additional degree of freedom, shown by rotational motion arrows 504to implant 300. It can be seen that by rotating implant 300 it can beimplanted on an asymmetrical vertebra, for example where the excision ofparts of the vertebra results in an asymmetrical implantation site forimplant 300, in an embodiment of the invention.

FIG. 5C is a cross-sectional view of rotation wedge 402 of a spinalimplant 300 with opposing components 304, 312 capable of rotating abouta vertical axis 502, in accordance with an exemplary embodiment of theinvention. Rotation wedge 402 is a part of non-sliding portion 304, inan embodiment of the invention. Wedge 402 is provided with angled faces506 which set the maximum rotational angle at which sliding portion 312can rotate with respect to non-sliding portion 304. In an embodiment ofthe invention, the maximum rotational angle up to 90 degrees.Optionally, the maximum rotational angle is up to 30 degrees. In anembodiment of the invention, a non-angled face 508 is provided tonon-sliding portion 504 to provide a base, non-rotated configuration forimplant 300.

FIG. 6 is an exploded view of a spinal implant 600 with a cam screwarrangement for interfacing with at least one rod 602 of a spinalimplant system, in accordance with an exemplary embodiment of theinvention. As described elsewhere herein, spinal implants 300, 600 areused as prosthetics to stand in for excised, altered, and/or damagedportions of the spinal column. Additionally and/or optionally and/oralternatively, spinal implants described herein are used as at least apart of a cross-linking system for stabilizing at least a portion of thespine by mechanically linking two or more vertebrae together. In anembodiment of the invention, at least one cam screw 604 is provided toimplant 600 which in nominal operation is rotatably positioned within ascrew hole 606. Screw hole 606 and cam screw 604 are relatively sized topermit the rotation of cam screw 604 within screw hole 606, but toprevent the passage of the cam end 608 of cam screw 604 from passingthrough screw hole 606. In an embodiment of the invention, a camretaining pin 610 is used to prevent the rotation tool interface end 612of cam screw 604 from passing through the screw hole 606 and/or toprovide a locking mechanism for the cam screw arrangement. The cam screwarrangement is described in more detail with respect to FIGS. 7A-7C and8.

In an embodiment of the invention, the implant 300, 600 is adapted toattach to a fusion rod at or near the spinous process. Optionally, thefusion rod at or around the spinous process 302 is the third fusion rodattached to the device. In an embodiment of the invention, a pluralityof fusion rod sizes are accommodated, for example by providing a camscrew, such as those described elsewhere herein to the spinous process302 for securing the rod in place. Optionally, a clamp-like mechanism isused to secure the rod to the device. Optionally, a tightening screwtraps the rod against an immovable bracket to secure the rod. In someembodiments of the invention, the rod attached at or near the spinousprocess is attached in the same location on an adjacent implant, that ison an implant on a vertebra adjacent. Optionally, the rod is attached toan implant on a non-adjacent vertebra.

FIG. 7A is a perspective view of implant 600 with a cam screwarrangement for interfacing with a rod 602 of a cross-link system, inaccordance with an exemplary embodiment of the invention. The cam screwarrangement features the ability to connect implant 600 to a pluralityof different sized (e.g. circumference) rods 602 by providing a camberedsurface 702 on the cam end 608 of cam screw 604 which graduallyreduces/increases (depending on direction of motion) in size across therange of motion of the screw 604, in accordance with an embodiment ofthe invention. Starting at the largest portion of the cambered surface702, the screw 604 is tightened until the rod 602 is securely connectedto the implant 600, being trapped between the cam screw 604 and thebracket portion 708 of the implant 600, allowing for rods 602 to be usedwith implant 600 which go from as large as the largest part of thecambered surface 702 to as small as the smallest part of the camberedsurface 702. Optionally, the rod is tightened in a clockwise direction.In some embodiments of the invention, size markings are provided on theimplant 600 and/or screw 604 to show to the attending medicalprofessional how much the screw 604 needs to be turned to properlysecure the rod 602 being used to the implant 600.

FIG. 7C is a cross-sectional view of implant 600, taken from thecross-section indicated in FIG. 7B, with a cam screw arrangement forinterfacing with a rod 602 of a cross-link system, in accordance with anexemplary embodiment of the invention. Seen in greater detail is thepositioning of fusion rod 602 with respect to cam screw 604, wherein thecambered surface 702 acts as a counterpart to the rod 602. Also shown ingreater detail is cam retaining pin 610, which in an embodiment of theinvention is located at least partially within a retaining pin groove704. Retaining pin groove 704 and cam retaining pin 610 are adapted toprovide at least one of the functions of mechanically preventing end 612from passing through screw hole 606 and providing a locking mechanism tothe cam screw arrangement. In an embodiment of the invention, camretaining pin 610 is rigid. In an embodiment of the invention, theretaining pin groove 704 extends around the circumference of rotationtool interface end 612.

In an embodiment of the invention, the cam retaining pin is providedwith clearance from the cam screw so that the cam screw can rotatefreely but is still prevent from passing through screw hole 606.

The locking mechanism function is provided by adapting retaining pingroove 704 with a locking point 706 which is sized and shaped so that asthe cam screw 604 is intentionally rotated, the retaining pin 610 isimpinged and/or crossed over the locking point 706 whereby once on theother side of the locking point 706 back rotation of the cam screw 604is inhibited, absent intentional back rotational force applied to thecam screw 604.

In an embodiment of the invention, the cam retaining pin is positionedto interface with the cam retaining groove. Optionally, the retainingpin groove 704 is provided with a plurality of locking points, seriallyarranged in the groove 704. Additionally and/or optionally, the lockingpoints are located in the retaining pin groove 704 to correspond tocommercially available and/or commonly used rod sizes such that at leastone locking point is provided for each size. In an embodiment of theinvention, as the cam screw 604 is turned it “locks” repetitively whereback rotation is inhibited up to and including the final locking whenthe cambered surface 702 size matches the rod size and wherein thelocking point placed in the retaining pin groove to match that rod sizeis traversed.

In an embodiment of the invention the cam retaining pin 610 is flexible.Optionally, the cam retaining pin 610 is constructed of rubber,stainless steel, or a polymer, for example PEEK. In some embodiments ofthe invention, the polymer is biodegradable. Optionally, the polymer isnon-biodegradable.

It should be noted that in an embodiment of the invention, fusion rodswhich are not perfectly parallel, as attached to the patient's spine,can still be used in conjunction with the implants described hereinwhich have the width and/or orientation adapting features. Non-parallelrods will increase or decrease distance from each other at a set angleas you move up or down the spine. By using the adjustable width and/orthe adjustable orientation features of the implants described herein, asingle implant model can be used, rather than having a plurality ofindividually specialized implants designed to accommodate non-parallelrods.

The spinal implants described herein 300, 600 also accommodate for sizedifferences amongst individual vertebral segments, in an embodiment ofthe invention. For instance, size variability within the cervical spine.A feature of implant 600 relative to its configuration is that as across-link, its generally triangular geometry reduces the risk ofimpingement on the spinal cord and/or thecal sac. This is contrast toexisting cross-links which are straight, wherein there is a risk ofimpingement. Therefore, the traditional cross-links cannot always beused. It is noted that other spinal implants described herein alsopossess triangular geometry.

FIG. 8 is a perspective view of cam screw 604 used in a cam screwarrangement for interfacing with rod 602 of a cross-link system, inaccordance with an exemplary embodiment of the invention. Shown in moredetail is the cambered surface 702 of cam screw, as well as theretaining pin groove 704, which in this figure does not show any lockingpoints 706. Optionally, no locking points 706 are used.

In an embodiment of the invention, the cambered surface 702 of the camscrew is adapted to interface with commonly used rod sizes, for exampleranging from 3.3 mm to 5.0 mm. It should be understood, however, thatthe cam screw could be adapted with a camber to match almost any rodsize which is usable for a cross-linking system.

In an embodiment of the invention, spinal implant 300, 600 is adapted tobe used with a spring screw, for example as described in related patentapplication entitled Spring Screw Apparatus and Methods of Using Same,filed on the same date as this application. Spinal implant 300 isprovided with a flange around the at least one loop 310 which acts as acounterpart to a spring located on the screw to lock the spring in theplane of the flange such that as the spring screw is tightened theimplant 300 tightens to the vertebra.

FIG. 9A is a perspective view of a damaged spinal column 100 with aspinal implant 300, 600 implanted thereon, in accordance with anexemplary embodiment of the invention. It can be seen that a pluralityof spinal implants 300, 600 on consecutive vertebrae can becross-linked, shown in FIG. 9B and as described herein, in someexemplary embodiments of the invention.

FIG. 10A is a cross-sectional view of a modified cervical vertebra 1002with spinal implant 300 implanted thereon, in accordance with anexemplary embodiment of the invention. In the exemplary embodimentshows, implant 300 is attached to a vertebra 1002 at the inferiorarticular process 1010 and functions as a lamina prosthetic. It shouldbe understood with respect to FIG. 10A and FIGS. 10B-10C below, thatdepending on the condition of the patient different parts of thevertebra may need to be replaced and therefore, implant 300 is attachedaccordingly. For example, in an embodiment of the invention, implant 300is attached to the vertebra at the pedicles. In some embodiments of theinvention, implant 300 is attached at a facet or what is left of alamina after a partial laminectomy. In some embodiments of theinvention, one side of the implant is attached to a different anatomicalpart than the other side of the implant or at a different correspondinglocation on the same anatomical part.

FIG. 10B is a cross-sectional view of a modified thoracic vertebra 1004with spinal implant 300 implanted thereon, in accordance with anexemplary embodiment of the invention.

FIG. 10C is a cross-sectional view of a modified lumbar vertebra 1006with spinal implant 300 implanted thereon, in accordance with anexemplary embodiment of the invention.

FIG. 11 is a flowchart 1100 showing a method of implanting spinalimplant 300, 600 at an implant site, in accordance with an exemplaryembodiment of the invention. Spinal implant 300, 600 is adjusted (1102)to fit a specific vertebral anatomy at an implant site and/or for use ina cross-linking arrangement over a plurality of vertebrae by anattending medical professional who is either performing or assisting theperformance of the implantation procedure, in an embodiment of theinvention. In an embodiment of the invention, spinal implant 300, 600 isadjusted by rotating (1104) and/or sliding (1106) at least a portion ofthe implant with respect to another portion of the implant such that thedesired length and/or orientation of the implant is achieved. In anembodiment of the invention, control of the sliding and/or rotating isselectively variable across a spectrum from moving freely to lockeddepending on the degree the screw is tightened.

In an embodiment of the invention, screws are passed through the loops306 and screwed at the fastening locations into the vertebra 200 tosecure (1108) spinal implant 300, 600. The screws can be placed in alateral mass, facet, lamina and/or pedicle of the bone, in an embodimentof the invention.

In some embodiments of the invention, spinal implant 300 is connectedand/or is a component of a cross-linking system whereby the implant isconnected to at least one rod 602 which is in turn connected to at leastone vertebra such that the rod traverses the implant site. In anembodiment of the invention, at least one cross-link rod is fastened(1110) to the spine and then at least one spinal implant is connected(1112) to the rod. Alternatively, the implant is connected first to therod and then the rod is fastened to the spine.

FIG. 12 is a flowchart 1200 showing a method for enabling attachment ofa spinal implant 600 to a plurality of different sized cross-link rods,in accordance with an exemplary embodiment of the invention. In anembodiment of the invention, the fusion rod 602 is fastened (1202) to atleast one vertebra. In an embodiment of the invention, fastening (1202)is performed in any one of the known methodologies. At least one spinalimplant 600 is placed (1204) over the rod 602 such that bracket 708receives the rod 602 between the bracket 708 and the cam screw 604. Inan embodiment of the invention, at least one spinal implant is placed(1204) over the pre-attached cross-link rod using the adjustmentfeatures of the spinal implant, including sliding and/or rotating. In anembodiment of the invention, when the spinal implant is placed (1204)over the cross-link rod, the cam screw 604 which is provided to thespinal implant is in an “open” position, wherein the cambered surface702 of the cam screw 604 is not yet engaged with the rod 602.

In an embodiment of the invention, placement (1204) of the implant 600includes adjusting the implant 600 width by sliding and/or adjusting theimplant orientation by rotating, as described elsewhere herein.

The cam screw 604 is tightened (1206) until the rod 602 is securelyconnected (1208) to the spinal implant 600 by pinning the rod betweenthe cam screw 604 and the bracket portion 708, in an embodiment of theinvention. Optionally, connecting (1208) is enhanced by providing atleast one locking position to the cam screw 604 such that as cam screw604 is tightened (1206), cam retaining pin 610 traverses a protrusion inthe retaining pin groove 704 which prevents back-rotation of the camscrew 604 (establishing a “locking point”), absent intentionally appliedback-driving force. Optionally, the locking position is adapted tocorrespond to a specific cross-link rod size, for example one that ispopularly used and/or readily commercially available. In someembodiments of the invention, where a plurality of locking positions areprovided to cam screw 604 retaining pin groove 704, the cam screw 604 istightened (1206) to the locking position which is closest to and/orwhich was specifically placed for the cross-link rod being connected(1208) to. Thus, in some embodiments of the invention, tightening (1206)includes traversing at least one locking point to arrive at theappropriately placed locking point for best fit. The process ofattaching implants to the vertebrae for use in a cross-linkingarrangement is repeated (1210) depending on how many vertebrae are beingcross-linked together, in an exemplary embodiment of the invention.

Unless otherwise defined, all technical and/or scientific terms usedherein have the same meaning as commonly understood by one of ordinaryskill in the art to which the invention pertains. Although methods andmaterials similar or equivalent to those described herein can be used inthe practice or testing of embodiments of the invention, exemplarymethods and/or materials are described below. In case of conflict, thepatent specification, including definitions, will control. In addition,the materials, methods, and examples are illustrative only and are notintended to be necessarily limiting.

The terms “comprises”, “comprising”, “includes”, “including”, “having”and their conjugates mean “including but not limited to”. This termencompasses the terms “consisting of” and “consisting essentially of”.

The phrase “consisting essentially of” means that the composition ormethod may include additional ingredients and/or steps, but only if theadditional ingredients and/or steps do not materially alter the basicand novel characteristics of the claimed composition or method.

As used herein, the singular form “a”, “an” and “the” include pluralreferences unless the context clearly dictates otherwise. For example,the term “a compound” or “at least one compound” may include a pluralityof compounds, including mixtures thereof.

Throughout this application, various embodiments of this invention maybe presented in a range format. It should be understood that thedescription in range format is merely for convenience and brevity andshould not be construed as an inflexible limitation on the scope of theinvention. Accordingly, the description of a range should be consideredto have specifically disclosed all the possible subranges as well asindividual numerical values within that range. For example, descriptionof a range such as from 1 to 6 should be considered to have specificallydisclosed subranges such as from 1 to 3, from 1 to 4, from 1 to 5, from2 to 4, from 2 to 6, from 3 to 6 etc., as well as individual numberswithin that range, for example, 1, 2, 3, 4, 5, and 6. This appliesregardless of the breadth of the range.

Whenever a numerical range is indicated herein, it is meant to includeany cited numeral (fractional or integral) within the indicated range.The phrases “ranging/ranges between” a first indicate number and asecond indicate number and “ranging/ranges from” a first indicate number“to” a second indicate number are used herein interchangeably and aremeant to include the first and second indicated numbers and all thefractional and integral numerals therebetween.

As used herein the term “method” refers to manners, means, techniquesand procedures for accomplishing a given task including, but not limitedto, those manners, means, techniques and procedures either known to, orreadily developed from known manners, means, techniques and proceduresby practitioners of the chemical, pharmacological, biological,biochemical and medical arts.

As used herein, the term “treating” includes abrogating, substantiallyinhibiting, slowing or reversing the progression of a condition,substantially ameliorating clinical or aesthetical symptoms of acondition or substantially preventing the appearance of clinical oraesthetical symptoms of a condition.

It is appreciated that certain features of the invention, which are, forclarity, described in the context of separate embodiments, may also beprovided in combination in a single embodiment. Conversely, variousfeatures of the invention, which are, for brevity, described in thecontext of a single embodiment, may also be provided separately or inany suitable subcombination or as suitable in any other describedembodiment of the invention. Certain features described in the contextof various embodiments are not to be considered essential features ofthose embodiments, unless the embodiment is inoperative without thoseelements.

Although the invention has been described in conjunction with specificembodiments thereof, it is evident that many alternatives, modificationsand variations will be apparent to those skilled in the art.Accordingly, it is intended to embrace all such alternatives,modifications and variations that fall within the spirit and broad scopeof the appended claims.

All publications, patents and patent applications mentioned in thisspecification are herein incorporated in their entirety by referenceinto the specification, to the same extent as if each individualpublication, patent or patent application was specifically andindividually indicated to be incorporated herein by reference. Inaddition, citation or identification of any reference in thisapplication shall not be construed as an admission that such referenceis available as prior art to the present invention. To the extent thatsection headings are used, they should not be construed as necessarilylimiting.

Those familiar with spinal implants will appreciate that manymodifications and substitutions can be made to the foregoing preferredembodiments of the present invention without departing from the spiritand scope of the present invention, defined by the appended claims.

1. An adjustable spinal implant device, comprising: a sliding portionprovided with a tongue; and, a non-sliding portion provided with a slotadapted for receipt of the tongue; wherein the tongue is slidably androtatably positioned within the slot.
 2. An adjustable spinal implantdevice according to claim 1, wherein a screw hole is provided to thenon-sliding portion adapted for receipt of a tightening screw therein.3. An adjustable spinal implant device according to claim 2, wherein thetightening screw defines an axis for rotation of the sliding andnon-sliding portions with respect to each other.
 4. An adjustable spinalimplant device according to claim 2, wherein a sliding track locatedwithin the tongue is adapted for receipt of the tightening screw.
 5. Anadjustable spinal implant device according to claim 1, furthercomprising a prosthetic spinous process.
 6. An adjustable spinal implantdevice according to claim 5, further comprising at least one soft tissueattachment hole located on the prosthetic spinous process.
 7. Anadjustable spinal implant device according to claim 1, furthercomprising at least one loop adapted for receipt of a bone screwtherethrough on the anterior of at least one of the sliding portion andthe non-sliding portion.
 8. An adjustable spinal implant deviceaccording to claim 1, further comprising at least one cam screw bracketadapted for receipt of a cam screw therethrough on the anterior of atleast one of the sliding portion and the non-sliding portion.
 9. Anadjustable spinal implant device according to claim 8, wherein the camscrew is provided with a tapered and cambered surface.
 10. An adjustablespinal implant device according to claim 9, wherein the tapered andcambered surface tapers from large to small in the tightening rotationaldirection.
 11. An adjustable spinal implant device according to claim 9,wherein the tapered and cambered surface is a counterpart to the outercircumference of a plurality of fusion rods.
 12. An adjustable spinalimplant device according to claim 8, wherein the cam screw is providedwith a cam retaining pin groove.
 13. An adjustable implant deviceaccording to claim 12, wherein the cam retaining pin groove is providedwith at least one locking point.
 14. An adjustable spinal implant deviceaccording to claim 1, wherein the spinal implant is between 20.0 mm to45.0 mm in the anterior/posterior axis, between 10.0 mm to 30.0 mm inthe superior/inferior axis, and between 25.0 mm to 55.0 mm in thedextro/sinistral axis.
 15. An adjustable spinal implant device accordingto claim 14, wherein the spinal implant is adapted for use with cervicalvertebrae and is between 20.0 mm to 30.0 mm in the anterior/posterioraxis, 10.0 mm to 20.0 mm in the superior/inferior axis and 25.0 mm to35.0 mm in the dextro/sinistral axis.
 16. An adjustable spinal implantdevice according to claim 14, wherein the spinal implant is adapted foruse with thoracic vertebrae and is 25.0 mm to 35.0 mm in theanterior/posterior axis, 15.0 mm to 25.0 mm in the superior/inferioraxis and 35.0 mm to 45.0 mm in the dextro/sinistral axis.
 17. Anadjustable spinal implant device according to claim 14, wherein thespinal implant is adapted for use with lumbar vertebrae and is 35.0 mmto 45.0 mm in the anterior/posterior axis, 20.0 mm to 30.0 mm in thesuperior/inferior axis and 45.0 mm to 55.0 mm in the dextro/sinistralaxis.
 18. An adjustable spinal implant device according to claim 14,wherein the spinal implant is adapted for use with the thoracolumbarsection of the spine and is between 25.0 mm to 45.0 mm in theanterior/posterior axis, between 15.0 mm to 30.0 mm in thesuperior/inferior axis and between 35.0 mm to 55.0 mm in thedextro/sinistral axis.
 19. An adjustable spinal implant according toclaim 1, wherein the implant is at least partially constructed oftitanium.
 20. An adjustable implant according to claim 1, wherein theimplant is at least partially constructed of stainless steel.
 21. Anadjustable spinal implant according to claim 1, wherein the implant isat least partially constructed of polyetheretherketone.
 22. A cross-linksystem adapted for use with a plurality of fusion rod sizes, comprising:at least one fusion rod; at least one spinal implant provided with atleast one bracket located on the anterior of the implant; and, at leastone cam screw inserted through the at least one bracket and providedwith a tapered and cambered surface wherein the cambered surface tapersacross a spectrum corresponding to a plurality of outer circumferencesof a plurality of fusion rods.
 23. A cross-link system according toclaim 22, wherein the cambered surface is adapted to selectively trapthe at least one fusion rod between the cam screw and the bracket.
 24. Across-link system according to claim 22, wherein the at least one spinalimplant is provided with two portions which are slidable and rotatablein relation to each other to assist with positioning the cam screwagainst the at least one fusion rod.
 25. A cross-link system accordingto claim 22, wherein the taper of the cambered surface narrows in thetightening rotational direction.
 26. A cross-link system according toclaim 22, wherein the plurality of outer circumferences of a pluralityof fusion rods ranges from 3.3 mm to 5.0 mm.
 27. A locking cam screw,comprising, a cambered surface on a cam end; and, a retaining pin groovelocated around the circumference of a rotation tool interface endopposite the cam end on the cam screw; wherein the retaining pin grooveis provided with at least one locking point adapted to pass a retainingpin therethrough in at least a tightening direction.
 28. A locking camscrew according to claim 27, wherein the at least one locking point is anarrowing of the retaining pin groove.
 29. A locking cam screw accordingto claim 27, wherein the position of the at least one locking point inthe retaining pin groove relates to the rotational distance of cam screwneeded to match the cambered surface to the outer circumference of across-link rod.
 30. A locking cam screw according to claim 27, whereinthe retaining pin groove is provided with a plurality of locking points.31. A locking cam screw according to claim 30, wherein each of theplurality of locking points corresponds to a rotational distance neededto match the cambered surface to an outer circumference of a cross-linkrod.
 32. A method for implanting a spinal implant at an implant site,comprising: adjusting the spinal implant to the implant site by at leastone of sliding and rotating at least a first portion with respect to asecond portion of the implant; and, securing the spinal implant to theimplant site.
 33. A method according to claim 32, further comprisingfastening at least one cross-link rod so that is traverses the implantsite.
 34. A method according to claim 33, further comprising connectingthe implant to the at least one cross-link rod.
 35. A method accordingto claim 32, wherein the implant site includes at least one of apedicle, a facet, a lateral mass and a lamina.
 36. A method according toclaim 32, further comprising tightening a screw to selectively limit atleast one of sliding and rotating.
 37. A method for connecting at leastone spinal implant to at least one of a plurality of cross-link rods ina cross-link arrangement, comprising: connecting at least one cross-linkrod to a plurality of vertebrae; placing at least one spinal implantover the at least one cross-link rod wherein a cambered surface of a camscrew provided to the spinal implant is in the open position andproximal to the cross-link rod; and, tightening the cambered and taperedcam screw so that it engages the cross-link rod and pins it between thecam screw and the spinal implant.
 38. A method according to claim 37,further comprising repeating placing and tightening for additionalspinal implants and cross-link rods.
 39. A method according to claim 37,wherein placing includes at least one of sliding and rotating at least aportion of the spinal implant.
 40. A method according to claim 37,wherein at least two consecutive vertebrae are connected.
 41. A methodaccording to claim 37, wherein at least two non-consecutive vertebraeare connected.
 42. A method according to claim 37, further comprisinglocking the cam screw to inhibit back rotation of the cam screw.